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The combination treatment reduced prostate size and improved testosterone deficiency symptoms but was less effective for sexual function.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

The debate over density remains unresolved.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

A new genetic mutation was found causing hair and eye issues in a boy.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

The document's conclusion cannot be provided because the text is not in a processable format.

The AC 2 peptide from Trapa japonica fruit helps protect hair cells and may treat hair loss.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

VDC-1101 shows potential as a treatment for canine cutaneous T-cell lymphoma.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

The man has Temporal Triangular Alopecia, a stable, non-scarring hair loss condition best treated with hair transplantation.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

The impact of virtual care on health and privacy is unclear and may be biased.

GhDET2 is crucial for cotton fiber growth.

LED light therapy at 863 nm wavelength can slow down skin tumor growth and reduce inflammation in mice.

Hair-Thread Tourniquet Syndrome is a rare condition where hair or thread tightly wraps around a child's body part, requiring quick treatment to prevent damage.

The procedure accurately measures 5-alpha-dihydrotestosterone in blood, useful for standard tests.

The new automatic tool accurately measures hair thickness and is reliable.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.